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01 6SANOFI AVENTIS US

02 2MANKIND PHARMA

03 2ABBOTT

04 2AIPING PHARM INC

05 2AJANTA PHARMA LTD

06 2ALEMBIC

07 4ALKEM LABS LTD

08 2AMNEAL PHARMS CO

09 4ANI PHARMS

10 2APPCO

11 2ASCOT

12 2AUROBINDO PHARMA USA

13 2AZURITY

14 2BARR LABS INC

15 3BOEHRINGER INGELHEIM

16 2CASPER PHARMA LLC

17 2CHARTWELL RX

18 1COSETTE

19 2DAVA PHARMS INC

20 2INVENTIA

21 2IPCA LABS LTD

22 3IVAX PHARMS

23 2KV PHARM

24 1MONARCH PHARMS

25 5MUTUAL PHARM

26 2MYLAN

27 3NATCO PHARMA

28 2NOSTRUM LABS

29 2NOVARTIS

30 2NOVAST LABS

31 2NOVITIUM PHARMA

32 3PAR PHARM

33 2PHARMOBEDIENT

34 1PIONEER PHARMS

35 2PLIVA

36 1PRM PHARMA LLC

37 2PUREPAC PHARM

38 1SANDOZ

39 4SUN PHARM INDUSTRIES

40 2SUNNY

41 2SUPERPHARM

42 4TWI PHARMS

43 2UMEDICA

44 4UNICHEM

45 2USL PHARMA

46 2VANGARD

47 2WARNER CHILCOTT

48 7WATSON LABS

49 4ZYDUS PHARMS

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : Yes

TE Code :

CHLORTHALIDONE

Brand Name : HYGROTON

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 12283

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Sanofi Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code : AB

CHLORTHALIDONE

Brand Name : CHLORTHALIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Approval Date : 2022-08-04

Application Number : 215587

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : Yes

TE Code :

CHLORTHALIDONE

Brand Name : HYGROTON

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 12283

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Sanofi Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : No

TE Code :

CHLORTHALIDONE; RESERPINE

Brand Name : REGROTON

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG;0.25MG

Approval Date : 1982-01-01

Application Number : 15103

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Sanofi Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : No

TE Code :

CHLORTHALIDONE; RESERPINE

Brand Name : DEMI-REGROTON

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG;0.125MG

Approval Date : 1982-01-01

Application Number : 15103

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Sanofi Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : No

TE Code :

BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE

Brand Name : KERLEDEX

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG;12.5MG

Approval Date : 1992-10-30

Application Number : 19807

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Sanofi Company Banner

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : No

TE Code :

BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE

Brand Name : KERLEDEX

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG;12.5MG

Approval Date : 1992-10-30

Application Number : 19807

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Sanofi Company Banner

08

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code : AB

CHLORTHALIDONE

Brand Name : CHLORTHALIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Approval Date : 2022-08-04

Application Number : 215587

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Company Banner

09

ELCC
Not Confirmed
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ELCC
Not Confirmed

CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE

Brand Name : COMBIPRES

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG;0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 17503

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

10

ELCC
Not Confirmed
arrow
arrow
ELCC
Not Confirmed

CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE

Brand Name : COMBIPRES

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG;0.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 17503

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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